Global Patent Index - EP 1081225 A1

EP 1081225 A1 20010307 - Transgenic animal model for neurodegenerative diseases

Title (en)

Transgenic animal model for neurodegenerative diseases

Title (de)

Transgenes Tiermodel für neurodegenerative Erkrankungen

Title (fr)

Modèle animal transgénique de maladies neurodégénératives

Publication

EP 1081225 A1 20010307 (EN)

Application

EP 99116766 A 19990830

Priority

EP 99116766 A 19990830

Abstract (en)

The present application refers to a mouse parkin2 DNA- and protein sequence, containing mutations or deletions causing Parkinson's disease in a human if occurring in the according human sequence, the construction of a transgenic non-human animal containing such a mutated DNA sequence and therefore expressing no or a less active or non-active parkin protein as well as the use of this transgenic animal as a model for neurodegenerative diseases. <IMAGE> <IMAGE>

IPC 1-7

C12N 15/12; C12N 5/10; C12N 1/21; C12N 1/19; C07K 14/47; A01K 67/027; A61K 49/00; C12Q 1/68

IPC 8 full level

A01K 67/02 (2006.01); A01K 67/027 (2006.01); A61K 49/00 (2006.01); C07K 14/47 (2006.01); C12N 1/15 (2006.01); C12N 1/19 (2006.01); C12N 1/21 (2006.01); C12N 5/10 (2006.01); C12N 9/00 (2006.01); C12N 15/09 (2006.01); C12N 15/12 (2006.01); C12N 15/85 (2006.01); C12Q 1/68 (2006.01)

CPC (source: EP)

A61K 49/0008 (2013.01); C12N 9/93 (2013.01); C12N 15/8509 (2013.01); A01K 2207/15 (2013.01); A01K 2217/00 (2013.01); A01K 2217/05 (2013.01); A01K 2217/075 (2013.01); A01K 2267/03 (2013.01); A01K 2267/0318 (2013.01)

Citation (search report)

  • [Y] WO 9859050 A1 19981230 - US HEALTH [US], et al
  • [DY] DATABASE EMROD E.M.B.L. Databases; 13 July 1999 (1999-07-13), SHIMIZU N ET AL: "Mus musculus mRNA for parkin, complete cds", XP002131476
  • [DY] KITADA ET AL: "Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism", NATURE,GB,MACMILLAN JOURNALS LTD. LONDON, vol. 392, no. 6676, 9 April 1998 (1998-04-09), pages 605 - 608, XP002108469, ISSN: 0028-0836 & WO 9940191 A1 19990812 - SHIMIZU NOBUYOSHI [JP], et al
  • [DY] LÜCKING ET AL: "Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism", LANCET THE,GB,LANCET LIMITED. LONDON, vol. 352, no. 9137, 24 October 1998 (1998-10-24), pages 1355 - 1356, XP002108466, ISSN: 0140-6736
  • [DY] HATTORI ET AL: "Point Mutations (Thr240Arg and Ala311Stop) in the Parkin Gene", BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,US,ACADEMIC PRESS INC. ORLANDO, FL, vol. 249, no. 3, 1998, pages 754 - 758, XP002108468, ISSN: 0006-291X
  • [DY] LEROY ET AL: "Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease", HUMAN GENETICS,DE,BERLIN, vol. 103, no. 4, October 1998 (1998-10-01), pages 424 - 427, XP002108470
  • [DY] ABBAS ET AL: "A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe", HUMAN MOLECULAR GENETICS,GB,OXFORD UNIVERSITY PRESS, SURREY, vol. 8, no. 4, April 1999 (1999-04-01), pages 567 - 574, XP002108471, ISSN: 0964-6906
  • [DY] HATTORI N ET AL: "Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals", ANN NEUROL., vol. 44, no. 6, December 1998 (1998-12-01), pages 935 - 941, XP000877155

Designated contracting state (EPC)

AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

DOCDB simple family (publication)

EP 1081225 A1 20010307; AT E396263 T1 20080615; CA 2383564 A1 20010308; DE 60038966 D1 20080703; EP 1208200 A2 20020529; EP 1208200 B1 20080521; ES 2304973 T3 20081101; JP 2003512026 A 20030402; WO 0116176 A2 20010308; WO 0116176 A3 20010927

DOCDB simple family (application)

EP 99116766 A 19990830; AT 00956461 T 20000818; CA 2383564 A 20000818; DE 60038966 T 20000818; EP 0008071 W 20000818; EP 00956461 A 20000818; ES 00956461 T 20000818; JP 2001520735 A 20000818